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rs1549738

From SNPedia

Orientationminus
Stabilizedminus
Make rs1549738(C;C)
Make rs1549738(C;T)
Make rs1549738(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position217253999
is asnp
is mentioned by
dbSNPrs1549738
ebirs1549738
HLIrs1549738
Exacrs1549738
Varsomers1549738
Maprs1549738
PheGenIrs1549738
hapmaprs1549738
1000 genomesrs1549738
hgdprs1549738
ensemblrs1549738
gopubmedrs1549738
geneviewrs1549738
scholarrs1549738
googlers1549738
pharmgkbrs1549738
gwascentralrs1549738
openSNPrs1549738
23andMers1549738
23andMe allrs1549738
SNP Nexus

SNPshotrs1549738
SNPdbers1549738
MSV3drs1549738
GWAS Ctlgrs1549738
GMAF0.2819
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1549738
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.726562
summary